CSCQ - QA Support Intern

At Bristol Myers Squibb, our employees often ask, "Who are you working for?" - a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Inspire and be inspired. We offer a variety of opportunities for undergraduate and post-graduate students to use your talent, skills, education and passion to help make an impact on patient's lives - all while growing your career and earning academic credit.

Our Internship Programme gives you a real opportunity to gain practical 'hands-on' experience, training and shadow the experts of your chosen field. It also provides you with insight into what it's like to work with us.

We will place you in a six, nine or twelve month Internship Programme depending on the requirements of your degree course. So, are you ready to embark on a new adventure? We can't wait to see what you're made of!

Activities you will be involved in during your placement as Clinical Supply Chain Quality (CSCQ) include:

• Support the Qualified Person disposition process for Investigational Medicinal Product (IMP) to clinical trials in the EU and ASIA/PAC.
• Supports Packaging & Labeling activities performed at EUCWH.
• Provides Quality Assurance support in the Use Date Extension process.
• Provides Quality Assurance support (GMP/GDP guidance and training) for CSO Regional Logistics.
• Support in a timely manner, the investigations of non-conformances and quality incidents. Resolves and documents into Quality Management System deviations or problems pertaining to the review of documents. Conducts appropriate follow-up as required. Tracks deviation, investigations and CAPAs.
• Prepares and reviews procedural documents as requested by supervisor.
• Contribute to improving and maintaining CSCQ QMS
• Prepare and approve supply chain flow maps, and product specification files.
• Supporting generation of/updates existing Quality Agreements.
• Adherence to BMS core behaviors
• Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements.
• Liaise with BMS Supply Chain and Quality colleagues to ensure that disposition lead times are consistently met.
• Support the site inspection readiness program for internal and external regulatory inspections.
• Support the progression of GMP documents within the Documentation Management System.
• Authoring, review and approval of QA-related procedures.
• Identify and implement continuous improvements within the QA group to support business processes and metrics.
• Engage in Quality Culture initiatives.

What Qualities Are We Looking For?

We are looking for highly motivated individuals who can collaborate in teams and have the willingness to learn.

• Chemical & Pharmaceutical Sciences, Pharmacy, Biomolecular & Biomedical Science or Pharmaceutical & Biomedical Chemistry discipline of study.
• Passionate about the biopharma sector and innovation in healthcare.
• Strong communication skills.
• Ability to work as a member of a team.
• Energetic, collaborative and dedicated.

We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.